Canonical Allele Identifier: CA2340604835

Gene: MED25

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49829812_49829813delinsTC , CM000681.2:g.49829812_49829813delinsTC	GRCh38
NC_000019.9:g.50333069_50333070delinsTC , CM000681.1:g.50333069_50333070delinsTC	GRCh37
NC_000019.8:g.55024881_55024882delinsTC	NCBI36
NG_017091.1:g.16534_16535delinsTC , LRG_368:g.16534_16535delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000593767.3:c.552_553delinsTC	ENSP00000470692.3:p.Ser184=
ENST00000312865.10:c.552_553delinsTC MANE Select	ENSP00000326767.5:p.Ser184=
ENST00000538643.5:c.181-699_181-698delinsTC	ENSP00000437496.1:n.181-699_181-698delinsTC
ENST00000595185.5:c.552_553delinsTC	ENSP00000470027.1:p.Ser184=
ENST00000612791.4:c.552_553delinsTC	ENSP00000479851.1:p.Ser184=
ENST00000612854.4:c.450+797_450+798delinsTC	ENSP00000482155.1:n.450+797_450+798delinsTC
ENST00000617849.4:c.158-927_158-926delinsTC	ENSP00000484882.1:n.158-927_158-926delinsTC
ENST00000618715.4:c.158-926_158-925delinsTC	ENSP00000480731.1:n.158-926_158-925delinsTC
ENST00000620467.4:c.552_553delinsTC	ENSP00000482659.1:p.Ser184=
ENST00000622402.4:c.146-6015_146-6014delinsTC	ENSP00000478074.1:n.146-6015_146-6014delinsTC
NM_030973.3:c.552_553delinsTC , LRG_368t1:c.552_553delinsTC	NP_112235.2:p.Ser184=
XM_011527353.1:c.552_553delinsTC	XP_011525655.1:p.Ser184=
NM_001378355.1:c.552_553delinsTC	NP_001365284.1:p.Ser184=
NM_030973.4:c.552_553delinsTC MANE Select	NP_112235.2:p.Ser184=